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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 65 South Asian ancestry trio cases, 63 South Asian ancestry trio controls.
The effect
The reported allele is A; the catalogue records no effect size
; p = 7 × 10−14.
Where it sits Chromosome 10, band 10q26.13 — a missense change in LHPP.
What each result means
A/ATwo copies of the version the research linked to Spina bifida. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/COne copy of the version the research linked to Spina bifida. That is a smaller link than two copies.
C/CNo copy of the version the research linked to Spina bifida. This is the starting point the study compared everyone against.
rs75426652 is a single position in the genome, in or near the LHPP gene. Published research associates it with spina bifida. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs75426652 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs75426652 come from?
GWAS Catalog, Birth defects research 2024, PMID:38526198. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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